The Stakeholder Benefits Of EHR eSource In Clinical Trials

Few advancements in clinical research have been as transformative as the integration of eSource Electronic Health Records (EHR). At OpenClinica, we're passionate about highlighting the profound advantages this integration brings to the table. Just ask the clinical research coordinator and project director spearheading an adaptive platform trial focused on repurposed therapeutics for severe infectious diseases. In a recent case study, "How EHR eSource Drives Efficiencies Across Sites and Sponsors," we delve into the remarkable time and cost savings achieved through EHR eSource integration.

For instance, Amy MK Rovitelli, a Critical Care Research Coordinator at the University of Rochester, demonstrated a staggering reduction in manual entry time—from 60 minutes to just five minutes—by leveraging eSource data. This monumental shift isn't just about saving time; it's about revolutionizing the way clinical trials operate. Let's explore how EHR eSource integration is reshaping the landscape of clinical research in 2024.